All Photos(2)
About This Item
Linear Formula:
Br2C6H3CHO
CAS Number:
Molecular Weight:
263.91
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
mp
84-88 °C (lit.)
functional group
aldehyde
bromo
SMILES string
Brc1cc(Br)cc(C=O)c1
InChI
1S/C7H4Br2O/c8-6-1-5(4-10)2-7(9)3-6/h1-4H
InChI key
ZLDMZIXUGCGKMB-UHFFFAOYSA-N
Related Categories
Application
Reactant involved in:
- Suzuki-Miyaura cross-coupling reactions
- Synthesis of blue fluorescent dye derivatives for organic light emitting diodes
- Sharpless kinetic resolution for the formation of Baylis-Hillman enal adducts
- Synthesis of podophyllotoxin mimetic pyridopyrazoles as anticancer agents
- Allylic alkylation
- Synthesis of C2-symmetric biphosphine ligand I
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Punit P Seth et al.
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Double-action haloketones: A super silyl group enabled the first highly diastereoselective Mukaiyama aldol reactions of α-chloro- and α-fluoroketones with a wide range of aldehydes, providing anti-β-siloxy-α-haloketones. This process is compatible with one-pot double-aldol methodology and allows for rapid access to
Synthesis and luminescence characteristics of conjugated dendrimers with 2, 4, 6-triaryl-1, 3, 5-triazine periphery.
Kim CK, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 44(1), 254-263 (2006)
Conformational Behavior of Conjugated Polymers With Oligo (phenylene vinylene) Side Chains.
Peeter H and Koeckelberghs G.
Macromolecular Chemistry and Physics, 214(5), 538-546 (2013)
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